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10:00am Thursday, 30 June 2022
11:30am Thursday, 30 June 2022
MedTech Forum
Hogan Lovells
Level 17, 20 Martin Place
Sydney, New South Wales 2000
Australia

MedTech professionals will have a rare opportunity to sit down with MedTech Europe's, Oliver Bisazza, Director of Regulatory Policy, to hear an update on European Medical Device Regulation (EU-MDR). Co-hosted by MTAA and Hogan Lovells, the event will provide an overview of the current EU MDR market and the potential impact this can have on Australian Manufacturers and Sponsors.

As this event is limited to a small group, there is opportunity to ask questions and network with Oliver and other attendees. Morning Tea and networking will run from 11:00 - 11:30am.

Who should attend?

Manufacturers, authorised representatives, importer, distributor, regulatory affairs or quality management professionals involved with medical devices.

Limited Placements

Placements are limited to 35 people with registrations closing on Thursday, 17 March 2022, 5:00pm. Registrations will close once 35 placements are filled.

Start time

Please note the start time is 10:00am. Please show up 15 minutes before so we can start on time.

COVID-19 Restrictions

MTAA requires all attendees to show proof of double-vaccination.

Proudly Hosted by


Date: 21 March 2022
Time: 10:00 - 11:00am. Attendees are asked to arrived 15 minutes before
Networking: 11:00 - 11:30am. Morning Tea provided.
Venue: Hogan Lovells, Level 17, 20 Martin Place, Sydney NSW 2022


Sold Out

Additional Information

Oliver Bisazza, Director of Regulatory Policy, MedTech Europe

Oliver leads the Industrial Policies department, which supports members in their implementation of the new and changing EU regulatory requirements, including but not limited to: legislation linked to the European Green Deal, the HTA Cooperation Regulation, in vitro Diagnostics Regulation and the Medical Devices Regulation.

His team strives to facilitate ‘technical implementation’ of regulations in place across the EU, and to communicate the positions of the MedTech Europe membership to the European Commission, the Member States, and other relevant authorities and stakeholder.

When not working on EU regulations, Oliver also coordinates the activities of MedTech Europe’s Cardiovascular Sector Group.

Prior to joining MedTech Europe, he worked at Medtronic as Director of Regulatory Policy for EMEA. In addition to this company experience, Oliver has had trade association roles in Brussels, at COCIR (the European association for the radiological, electromedical and healthcare IT industries) and at EDANA (the industry association for the nonwovens and related industries).

Oliver is a native speaker of English, and a dual national of Australia and Malta. When not working, he enjoys travel, spending time with his family, and rock-climbing.